IP Library Granted Patent US 8,282,942
Granted Patent B2
US 8,282,942 · App. 12/754,970 · Granted Oct 9, 2012

Patent

Assignee: Trustees of Dartmouth College
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Quick Facts
Patent No.
US 8,282,942
App. No.
12/754,970
Granted
Oct 9, 2012
Kind
B2
Abstract

The present invention provides attenuated Toxoplasma gondii knockout mutants of the de novo pyrimidine synthesis pathway and use of the same in vaccines and methods of providing an immune response and protecting a subject against infection by T. gondii and a non- T. gondii disease.

Claims (16)

1. A vaccine comprising an isolated, attenuated, pyrimidine auxotrophic Toxoplasma gondii KU80 knockout mutant with (a) a selectable marker integrated into the coding region of KU80 protein of SEQ ID NO: 2 so the KU80 protein activity is abolished and (b) a knockout mutation of a gene of the de novo pyrimidine synthesis pathway.

2. The vaccine of claim 1 , wherein the gene of the de novo pyrimidine synthesis pathway encodes carbamoyl phosphate synthetase II, aspartate transcarbamylase, dihydroorotase, dihydroorotase dehydrogenase, orotate phosphoribosyltransferase, or orotidine 5′-monophosphate decarboxylase.

3. The vaccine of claim 1 , wherein the mutant further comprises one or more nucleic acid molecules encoding exogenous proteins.

4. The vaccine of claim 3 , wherein the nucleic acid molecules replaces the coding region or promoter of the gene encoding KU80 protein or the gene of the de novo pyrimidine synthesis pathway.

5. The vaccine of claim 3 , wherein the exogenous protein is a non- Toxoplasma gondii antigen.

6. The vaccine of claim 5 , wherein the antigen is a bacterial, viral, fungal, parasitic or tumor antigen.

7. The vaccine of claim 3 , wherein the exogenous protein produces a non- Toxoplasma gondii antigen.

8. The vaccine of claim 7 , wherein the antigen is a lipid or polysaccharide.

9. The vaccine of claim 1 , wherein the mutant has been gamma-irradiated.

10. The vaccine of claim 5 , wherein the mutant has been gamma-irradiated.

11. The vaccine of claim 7 , wherein the mutant has been gamma-irradiated.

12. A method for generating an immune response comprising administering to a subject in need thereof an effective amount of a vaccine of claim 1 thereby generating an immune response to the vaccine.

13. The method of claim 12 , wherein the immune response is a natural granulocyte, neutrophil, macrophage, GR1+ macrophage, B cell, or T cell immune response.

14. The method of claim 13 , wherein the immune response is an anti-tumor T cell response.

15. A method for generating an immune response comprising administering to a subject in need thereof an effective amount of a vaccine of claim 5 thereby generating an immune response to the vaccine.

16. A method for generating an immune response comprising administering to a subject in need thereof an effective amount of a vaccine of claim 7 thereby generating an immune response to the vaccine.

Assignments (2)
CONFIRMATORY LICENSE Recorded Jan 19, 2011
From: DARTMOUTH COLLEGE
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 025764/0963 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 20, 2010
From: BZIK, DAVID J.; FOX, BARBARA A.
To: TRUSTEES OF DARTMOUTH COLLEGE
Reel/Frame 024257/0121 →
Continuity (5)
Continuation In Part 12394365 · Feb 27, 2009
Continuation In Part PCTUS2008081274 · Oct 27, 2008
Provisional Application 60983339 · Oct 29, 2007
Provisional Application 61057972 · Jun 2, 2008
Related Publication 20100203085A1 · Aug 12, 2010